Zinn KR, Chaudhuri TR, Szafran AA, O’Quinn D, Weaver C, Dugger K, Lamar D, Kesterson RA, Wang X, Frank SJ: Noninvasive bioluminescence imaging in small animals. ILAR J 2008, 49:103–115.PubMedCentralPubMedCrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions MJJ participated in study design, in vivo studies, data analysis, and manuscript drafting. CHA participated in study design, in vitro studies, data analysis, and manuscript drafting. HK and JWC participated in study design, and interpretation of data. IJC and SJ participated

in in vitro studies, and data analysis. YHK and HY participated in in vivo studies, and data acquisition. YlK participated in study design, in vivo studies, data analysis, and manuscript drafting, and critical revision of the manuscript. All authors read and approved the final manuscript. Funding This work was supported in part by the Basic Science Research Program find more through the

National Research SN-38 nmr Foundation of Korea funded by the Ministry of Education, Science and Technology (2011–0010250), and the Korean Health Technology R&D Project, Ministry of Health & Welfare, Republic of Korea (HI12C1148).”
“Background Pituitary adenomas (PAs) account for about 15% of intracranial tumors. Although PAs are mostly benign lesions, about 30-55% of them are confirmed to locally invasive, and some of them infiltrate dura, bone and sinuses, are designated highly 3-oxoacyl-(acyl-carrier-protein) reductase aggressive [1,2]. The conventional treatment of large pituitary adenomas consists of surgery, and radiotherapy when it is hard to achieve total resection. The use of additional radiotherapy is limited by the risk of radiation necrosis of surrounding structures. Thus, medication treatment, although unlikely to be curative immediately, might lead to certain clinically therapeutic effect, as a useful supplement [3]. Currently, first-line clinical medication for PAs generally consists of dopamine agonists (DAs), somatostatin

analogs (SSAs) or combinations [4]. Recently, some routine chemotherapeutics such as Temozolomide (TMZ) and Bevacizumab have been selleck inhibitor carefully studied to treat PAs and considered to be potential for aggressive PAs’ medical therapy [5-8]. DAs were widely used for the treatment of prolactinomas and some somatotropinomas, and the responsiveness depends on the expression of dopamine D2 receptors (D2R) on tumor cells. Abnormal expression of D2R in prolactinoma was considered to confer resistance to DA treatment. Fadul et al. [7] first reported two cases of pituitary carcinoma received TMZ treatment, concluding that TMZ may be effective in treating pituitary carcinomas. After that, more and more studies demonstrated the inspiring therapeutic effect of TMZ on pituitary carcinomas and aggressive PAs. As a DNA repairase, O6-methylguanine DNA methyltransferase (MGMT) confers chemoresistance to TMZ [9]. Thus, tumors with low expression of MGMT are usually sensitive to TMZ.